Muralidharan Arjun, Sotocinal Susana G, Austin Jean-Sebastien, Mogil Jeffrey S
Department of Psychology and Anesthesia, McGill University, Montreal, QC, Canada.
Pain Rep. 2020 May 29;5(3):e824. doi: 10.1097/PR9.0000000000000824. eCollection 2020 May-Jun.
Increasing attention is being paid to the effects of organismic factors like age on pain sensitivity. However, very little data exist on this topic using modern algesiometric assays and measures in laboratory rodents.
We investigated the effect of age and duration of nerve injury on baseline mechanical thresholds, neuropathic allodynia, and the antiallodynic and analgesic efficacy of 4 systemically administered analgesics: amitriptyline, diclofenac, morphine, and pregabalin.
Mice of both sexes and 3 conditions were compared: Young-Young, in which baseline testing (von Frey thresholds), the injury producing neuropathic pain (spared nerve injury [SNI]) and subsequent drug testing occurred while mice were young (8-10 weeks); Young-Old, in which mice received the nerve injury while young but were tested for drug efficacy over 10 months later; and Old-Old, in which both the nerve injury and drug testing occurred at approximately 1 year of age.
Old-Old mice were found to display higher baseline mechanical sensitivity than other groups. No group differences were seen in SNI-induced allodynia in males; female Young-Old mice were found to display greatly reduced allodynia. With respect to drug efficacy, no differences among conditions were observed for amitriptyline, diclofenac, or morphine. For pregabalin, however, Young-Old mice displayed significantly reduced antiallodynia, and the drug was completely ineffective in Old-Old mice.
Novel findings include the apparent remission of SNI-induced allodynia in female mice 10 months after injury and reduced pregabalin antiallodynic effects produced by both the passage of time after nerve injury and aging.
机体因素如年龄对疼痛敏感性的影响正受到越来越多的关注。然而,在实验室啮齿动物中,使用现代痛觉测量分析方法和指标研究该主题的数据非常少。
我们研究了年龄和神经损伤持续时间对基线机械阈值、神经性异常性疼痛以及四种全身给药镇痛药(阿米替林、双氯芬酸、吗啡和普瑞巴林)的抗异常性疼痛和镇痛效果的影响。
比较了两种性别和三种条件下的小鼠:年轻-年轻组,在小鼠年轻(8-10周)时进行基线测试(von Frey阈值)、产生神经性疼痛的损伤(保留神经损伤[SNI])以及随后的药物测试;年轻-老年组,小鼠在年轻时接受神经损伤,但在10个月后进行药物疗效测试;老年-老年组,神经损伤和药物测试均在约1岁时进行。
发现老年-老年组小鼠的基线机械敏感性高于其他组。雄性小鼠中,SNI诱导的异常性疼痛在各组之间没有差异;发现雌性年轻-老年组小鼠的异常性疼痛明显减轻。关于药物疗效,阿米替林、双氯芬酸或吗啡在不同条件下没有观察到差异。然而,对于普瑞巴林,年轻-老年组小鼠的抗异常性疼痛明显降低,并且该药物在老年-老年组小鼠中完全无效。
新发现包括损伤10个月后雌性小鼠中SNI诱导的异常性疼痛明显缓解,以及神经损伤后随着时间推移和衰老导致普瑞巴林抗异常性疼痛作用降低。